Purpose of the study
We reviewed 69 consecutive cases of total knee arthroplasty revisions to an
alyze the causes of failure.
Material and methods
Sixty-nine total knee arthroplasty revisions were required between 1990 and
1997 for non-septic failure. Five categories of failures were identified:
30 loosenings including 11 with an initial malposition (varus position of t
he tibial component in 8 cases), 14 laxities (medial in 5, lateral in 5 and
anteroposterior in 4), 11 stiff knees with no other clinical or radiologic
al anomaly, 6 patellar failures (2 dislocations, 2 cases of excessive wear,
2 painful knees with a Freeman prosthesis), and 8 cases of painful knees w
ith no other detectable anomaly.
Results
A three-phase reconstruction procedure was used after removing the failing
TKA: 1) reconstruction of the tibia with replacement of lost bone, 2) recon
struction of the femur with balanced flexion determining the size of the im
plant, 3) balanced extension determining the distal/proximal position of th
e femoral component. A "simple" sliding prosthesis was used in 16 cases, a
modular reconstruction prosthesis in 40 cases and a hinge prosthesis in 13
cases. Mean follow-up for functional and radiographic assessment after revi
sion surgery was 37 months (59 cases) with a minimum follow-up of 1 year. T
he best outcome was observed in the "loosening", "laxity", and "stiffness"
patients. Outcome was less favorable for the group "isolated pain" with IKS
functional scores of 35.5 +/- 16 and 52.5 +/- 21.
Discussion
In 36 p. 100 of cases, TKA failure was related to a technical mistake (comp
onent malposition, poor ligament alignment). In 33 p. 100, failure was pati
ent related (multiple procedures, congenital hip dysplasia, rheumatoid arth
ritis...). Outcome after revision TKA was less favorable than after primary
TKA, particularly in case of painful knees with no other detectable anomal
y.
Conclusion
Surgical revision of TKA must follow a rigorous procedure with a detailed p
reoperative work-up. The decision for revision must not be made unless a pr
ecise anomaly has been identified.